Description
1.
* Responsible for providing 'on-the-floor' technical support and trouble-shooting advice for manufacturing related issues including (but not limited to), Formulation, Equipment Preparation, Aseptic Filling, and Capping-related activities.
* 2.
* Make suggestions, recommendations, and contributions to process development and technically support all manufacturing activities for aseptically manufactured parenteral pharmaceutical products in a cGMP facility.
* 3.
* Individual will be responsible for conducting investigations and authoring Exception Reports related to manufacturing incidents, and helping to implement corrective and preventative action.
* 4.
* Individual will also assist with providing training to manufacturing and technical personnel and act as a liaison between the manufacturing operations and the project client (internal and external).
* 5.
* Responsible for preparation of technical reports, development of technical studies, providing input to the Quality Assurance department for product impact assessment, supporting internal and external audits, and supporting department initiatives.
* 6.
* Manage multiple projects with minimal supervision and willing to work weekends from time-to-time.
*
Requirements
1.
* Knowledge of the basic principles in various engineering and scientific disciplines.
* 2.
* Must be able to make quick reliable decisions under pressure.
*3.
* Must be a self-starter and able to work under minimal supervision in a fast-paced environment.
*4.
* Desire to learn basic pharmaceutical manufacturing principles and unit operations quickly.
* 5.
* Minimum of a BS in Engineering, Science, or Pharmaceutical-related field.
* 0 to 1 years required pharmaceutical experience.
*Percent Travel Required0%
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